Xist Intron 1 Repression by Transcriptional-Activator-Like Effectors Designer Transcriptional Factor Improves Somatic Cell Reprogramming in Mice

Stem Cells. 2019 May;37(5):599-608. doi: 10.1002/stem.2928. Epub 2019 Feb 21.

Abstract

Xist is the master regulator of X chromosome inactivation. In order to further understand the Xist locus in the reprogramming of somatic cells to induced pluripotent stem cells (iPSCs) and in somatic cell nuclear transfer (SCNT), we tested transcription-activator-like effectors-based designer transcriptional factors (dTFs), which were specific to numerous regions at the Xist locus. We report that the selected dTF repressor 6 (R6) binding the intron 1 of Xist, which caused higher H3K9me3 followed by X chromosome opening and repression of X-linked genes in mouse embryonic fibroblasts, rather than affecting Xist expression, substantially improved the iPSC generation and the SCNT preimplantation embryo development. Conversely, the dTF activator targeting the same genomic region of R6 decreased iPSC formation and blocked SCNT-embryo development. These results thus uncover the critical requirement for the Xist locus in epigenetic resetting, which is not directly related to Xist transcription. This may provide a unique route to improving the reprogramming. Stem Cells 2019;37:599-608.

Keywords: Xist intron 1; Induced pluripotent stem cells; Mouse embryonic fibroblast reprogramming; Somatic cell nuclear transfer; Transcriptional-activator-like effectors designer transcriptional factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cellular Reprogramming / genetics*
  • Embryonic Development / genetics
  • Epigenomics
  • Fibroblasts / cytology
  • Gene Expression Regulation, Developmental
  • Induced Pluripotent Stem Cells / cytology
  • Induced Pluripotent Stem Cells / metabolism
  • Introns / genetics
  • Mice
  • RNA, Long Noncoding / genetics*
  • Transcriptional Activation*
  • X Chromosome / genetics
  • X Chromosome Inactivation / genetics*

Substances

  • RNA, Long Noncoding
  • XIST non-coding RNA